Role and regulation of cyclooxygenase-2 during inflammation

医学 环氧合酶 炎症 萘丁美酮 止痛药 药理学 出血素质 免疫学 前列腺素 血小板 内科学 非甾体 生物化学 生物
作者
Lee S. Simon
出处
期刊:The American Journal of Medicine [Elsevier BV]
卷期号:106 (5): 37S-42S 被引量:390
标识
DOI:10.1016/s0002-9343(99)00115-1
摘要

Prostaglandins are formed from arachidonic acid by the action of cyclooxygenase (COX) and subsequent downstream synthetases. Recently, it has been found that there are two closely related forms of COX, which are now known as COX-1 and COX-2. Although both isoforms of this enzyme convert arachidonate to prostaglandins, there are significant differences in their distribution in the body and their roles in health and disease. The basis for these important differences lies in the genes for COX-1 and COX-2 and the regulation of these genes. COX-1, the predominantly constitutive form of the enzyme, is expressed throughout the body and provides certain homeostatic functions, such as maintaining normal gastric mucosa, influencing renal blood flow, and aiding in blood clotting by abetting platelet aggregation. In contrast, COX-2, the inducible form, is expressed in response to inflammatory and other physiologic stimuli and growth factors and is involved in the production of those prostaglandins that mediate pain and support the inflammatory process. All conventional nonsteroidal anti-inflammatory drugs (NSAIDs) nonspecifically inhibit both COX-1 and COX-2 at standard anti-inflammatory doses. The beneficial anti-inflammatory and analgesic effects occur through the inhibition of COX-2, but the gastrointestinal toxicities and the mild bleeding diathesis occur as a result of concurrent inhibition of COX-1. It is important that physicians fully understand the pharmacologic basis for the differential actions of NSAIDs when prescribing them for pain and inflammation. This understanding is also important so that physicians can critically evaluate the basis for, and the emerging data on, COX-2-specific inhibitors and their potential role in clinical medicine. Agents that would inhibit COX-2 while sparing COX-1 represent an attractive therapeutic development and could represent a major advance in the treatment of rheumatoid arthritis and osteoarthritis, as well as a diverse array of other conditions.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
愚者完成签到,获得积分10
1秒前
勤奋的天亦完成签到,获得积分10
1秒前
Zikc完成签到,获得积分10
2秒前
zhongcy完成签到,获得积分10
2秒前
2秒前
光亮的青文完成签到 ,获得积分10
4秒前
曾经耳机完成签到 ,获得积分10
5秒前
5秒前
阳光绿柏完成签到,获得积分10
6秒前
云哈哈完成签到,获得积分10
6秒前
优秀星星完成签到,获得积分10
7秒前
Monkey_Z完成签到,获得积分10
7秒前
小耿木木完成签到,获得积分10
8秒前
zyyyyyu完成签到,获得积分10
8秒前
笨笨西装完成签到,获得积分10
8秒前
9秒前
谨慎的安柏完成签到,获得积分10
9秒前
闾丘寻云完成签到,获得积分10
9秒前
实验大牛完成签到,获得积分10
10秒前
wxx完成签到,获得积分10
10秒前
玻尿酸完成签到,获得积分10
11秒前
11秒前
MiriamYu完成签到,获得积分10
11秒前
ccc发布了新的文献求助10
12秒前
MchemG应助枯叶蝶采纳,获得20
12秒前
hebnkygzs完成签到 ,获得积分10
14秒前
董雪发布了新的文献求助10
15秒前
噼里啪啦完成签到,获得积分10
16秒前
隐形的冰岚完成签到,获得积分10
16秒前
123完成签到,获得积分10
18秒前
Zsy完成签到,获得积分10
18秒前
清脆诗兰完成签到 ,获得积分10
18秒前
深情千雁完成签到,获得积分10
18秒前
xiaostou完成签到,获得积分10
19秒前
lbx完成签到,获得积分10
21秒前
cdercder应助Never stall采纳,获得10
21秒前
啊啊啊啊啊啊啊完成签到,获得积分10
22秒前
satellite完成签到,获得积分10
22秒前
Lou发布了新的文献求助10
23秒前
自然完成签到,获得积分10
23秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7298408
求助须知:如何正确求助?哪些是违规求助? 8916795
关于积分的说明 18879891
捐赠科研通 6963494
什么是DOI,文献DOI怎么找? 3210653
关于科研通互助平台的介绍 2379981
邀请新用户注册赠送积分活动 2187144